Signals transducers and activators of transcription (STAT)-induced STAT inhibitor-1 (SSI-1)/suppressor of cytokine signaling-1 (SOCS-1) suppresses tumor necrosis factor α-induced cell death in fibroblasts

被引:162
|
作者
Morita, Y
Naka, T
Kawazoe, Y
Fujimoto, M
Narazaki, M
Nakagawa, R
Fukuyama, H
Nagata, S
Kishimoto, T
机构
[1] Osaka Univ, Sch Med, Dept Med 3, Suita, Osaka 5650871, Japan
[2] Osaka Univ, Sch Med, Dept Microbiol, Suita, Osaka 5650871, Japan
[3] Osaka Univ, Sch Med, Dept Genet, Suita, Osaka 5650871, Japan
[4] Fujisawa Pharmaceut Co Ltd, Dept Immunol, Yodogawa Ku, Osaka 5328514, Japan
[5] Fujisawa Pharmaceut Co Ltd, Inflammat Med Biol Res Lab, Yodogawa Ku, Osaka 5328514, Japan
关键词
D O I
10.1073/pnas.090084797
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Signal transducers and activators of transcription (STAT)-induced STAT inhibitor-1 [SSI-1; also known as suppressor of cytokine signaling-1 (SOCS-1)] was identified as a negative feedback regulator of Janus kinase-STAT signaling. We previously generated mice lacking the SSI-1 gene (SSI-1 -/-) and showed that thymocytes and splenocytes in SSI-1 -/- mice underwent accelerated apoptosis. In this paper, we show that murine embryonic fibroblasts lacking the SSI-1 gene are more sensitive than their littermate controls to tumor necrosis factor-alpha (TNF-alpha)-induced cell death. In addition, L929 cells forced to express SSI-l (L929/SSI-1), but not SSI-3 or SOCS-5, are resistant to TNF-alpha-induced cell death. Furthermore L929/SSI-1 cells treated with TNF-alpha sustain the activation of p38 mitogen-activated protein (MAP) kinase. In contrast, SSI-1 -/- murine embryonic fibroblasts treated with TNF-alpha show hardly any activation of p38 MAP kinase. These findings suggest that SSI-1 suppresses TNF-alpha-induced cell death, which is mediated by p38 MAP kinase signaling.
引用
收藏
页码:5405 / 5410
页数:6
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